Q906
Quinizarin
96%
Sinônimo(s):
1,4-Dihydroxyanthraquinone
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About This Item
Fórmula empírica (Notação de Hill):
C14H8O4
Número CAS:
Peso molecular:
240.21
Beilstein:
1914036
Número CE:
Número MDL:
Código UNSPSC:
12352103
ID de substância PubChem:
NACRES:
NA.23
Produtos recomendados
densidade de vapor
8.3 (vs air)
pressão de vapor
1 mmHg ( 196.7 °C)
Ensaio
96%
pf
198-199 °C (lit.)
cadeia de caracteres SMILES
Oc1ccc(O)c2C(=O)c3ccccc3C(=O)c12
InChI
1S/C14H8O4/c15-9-5-6-10(16)12-11(9)13(17)7-3-1-2-4-8(7)14(12)18/h1-6,15-16H
chave InChI
GUEIZVNYDFNHJU-UHFFFAOYSA-N
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Aquatic Acute 1 - Aquatic Chronic 1
Código de classe de armazenamento
13 - Non Combustible Solids
Classe de risco de água (WGK)
WGK 2
Ponto de fulgor (°F)
431.6 °F
Ponto de fulgor (°C)
222 °C
Equipamento de proteção individual
Eyeshields, Faceshields, Gloves, type N95 (US)
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Anthracene (AC) is a non-mutagenic and non-carcinogenic, low-molecular-weight polycyclic aromatic hydrocarbon present in the environment. Its toxicity can be dramatically increased after solar-light exposure. Biotransformation capacities of AC by Tetrahymena pyriformis and a selection of eight micromycetes were studied, and
M M Fiallo et al.
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The interaction of Fe3+ with several anthracycline antitumour antibiotics has been reinvestigated. Absorption and circular dichroism (CD) measurements were carried out (i) in aqueous solution and (ii) in semi-aqueous MeOH to avoid the stacking of the anthracycline molecules. The Fe3+
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The effect of dihydroxyanthraquinone (DHAQ), a new antitumor drug, on mammalian chromosome replication was investigated using simian virus 40 (SV40) as a model system. The maximum effect of inhibition on viral DNA synthesis was observed within 30-40 min after the
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